Executive Director, CMC Program Management (Chemistry)
Company: Regeneron Pharmaceuticals, Inc.
Location: Troy
Posted on: January 2, 2026
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Job Description:
We are hiring an Executive Director to lead program management
for a portfolio of chemistry-based advanced therapies (ADC, siRNA,
mRNA, oligonucleotides, conjugates, peptides). Responsible for
end-to-end operational coordinationlinking Manufacturing, R&D,
CMC, clinical, regulatoryto enable accelerated development and
commercialization of advanced therapy treatments. In this role, a
typical day might include the following: Lead and develop a team of
610 program managers overseeing 2030 active programs across
clinical and commercial stages. Drive timeline acceleration and
optimization, balancing priorities across internal and external
manufacturing capacity, regulatory milestones, and resource
constraints. Work closely with clinical, development and
manufacturing teams to proactively identify and resolve development
and supply bottlenecks impacting clinical, regulatory or commercial
deliverables. Oversee clinical and commercial launch supply
readiness through coordination with internal teams and external
manufacturing group. Support data flow and documentation to enable
submissions by CMC regulatory teams, ensuring timely and complete
packages. Collaborate with Finance to inform investment needs and
help secure program budgets in a timely manner. Provide program
management leadership for tech transfers, manufacturing readiness,
and process scale-up. Coordinate post-launch activities including
lifecycle expansions, process improvements, and indication growth.
Establish governance tools, dashboards, and metrics for portfolio
visibility and decision-making. This role might be for you if you
have: Demonstrated success managing cross-functional timelines
under complex capacity, regulatory, and technical constraints.
Strong understanding of process chemistry, analytical development,
conjugation technologies, and tech transfer. Proven ability to
partner with scientists and engineers to drive efficient execution
and innovation. To be considered for this role you must hold a
Bachelors degree, with 18 years of experience in Biopharma
Operations, CMC, or Program Management with direct experience in
ADC, siRNA, or mRNA product development and successful launches, or
equivalent combination of education and experience. Ph.D. or M.S.
in Chemistry, Biochemistry, Chemical Engineering, or Pharmaceutical
Sciences preferred. Does this sound like you? Apply now to take
your first step towards living the Regeneron Way! We have an
inclusive culture that provides comprehensive benefits, which vary
by location. In the U.S., benefits may include health and wellness
programs (including medical, dental, vision, life, and disability
insurance), fitness centers, 401(k) company match, family support
benefits, equity awards, annual bonuses, paid time off, and paid
leaves (e.g., military and parental leave) for eligible employees
at all levels! For additional information about Regeneron benefits
in the US, please visit
https://careers.regeneron.com/en/working-at-regeneron/total-rewards/.
For other countries specific benefits, please speak to your
recruiter. Please be advised that at Regeneron, we believe we are
most successful and work best when we are together. For that
reason, many of Regenerons roles are required to be performed
on-site. Please speak with your recruiter and hiring manager for
more information about Regenerons on-site policy and expectations
for your role and your location. Regeneron is an equal opportunity
employer and all qualified applicants will receive consideration
for employment without regard to race, color, religion or belief
(or lack thereof), sex, nationality, national or ethnic origin,
civil status, age, citizenship status, membership of the Traveler
community, sexual orientation, disability, genetic information,
familial status, marital or registered civil partnership status,
pregnancy or parental status, gender identity, gender reassignment,
military or veteran status, or any other protected characteristic
in accordance with applicable laws and regulations. The Company
will also provide reasonable accommodation to the known
disabilities or chronic illnesses of an otherwise qualified
applicant for employment, unless the accommodation would impose
undue hardship on the operation of the Company's business. For
roles in which the hired candidate will be working in the U.S., the
salary ranges provided are shown in accordance with U.S. law and
apply to U.S.-based positions. For roles which will be based in
Japan and/or Canada, the salary ranges are shown in accordance with
the applicable local law and currency. If you are outside the U.S,
Japan or Canada, please speak with your recruiter about salaries
and benefits in your location. Please note that certain background
checks will form part of the recruitment process. Background checks
will be conducted in accordance with the law of the country where
the position is based, including the type of background checks
conducted. The purpose of carrying out such checks is for Regeneron
to verify certain information regarding a candidate prior to the
commencement of employment such as identity, right to work,
educational qualifications etc. Salary Range (annually) $239,600.00
- $399,400.00
Keywords: Regeneron Pharmaceuticals, Inc., Hamden , Executive Director, CMC Program Management (Chemistry), Manufacturing , Troy, Connecticut